[Re(Br)(CO)3]2(2,2'-bipyrimidine) | 128496-75-3

• 英文名称: [Re(Br)(CO)3]2(2,2'-bipyrimidine)
• 英文别名: anti-[Br(CO)₃Re(μ-2,2′-bipyrimidine)Re(CO)₃Br]；anti-[Br(CO)₃Re(μ-bpm)Re(CO)₃Br]；fac-{(μ-2,2-bipyrimidin)(tricarbonylrhenium)bromide}2
• CAS: 128496-75-3；170423-33-3
• 化学式: C₁₄H₆Br₂N₄O₆Re₂
• 分子量: 858.447
• InChiKey: DEVHPPBOOYEPRD-UHFFFAOYSA-L

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
  None
• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
  None
• 氢给体数：
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• 氢受体数：
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反应信息

• 作为产物：
  描述：

  bromotricarbonyl(tetrahydrofuran)rhenium(I) dimer 、 2 2'-联嘧啶 以 二氯甲烷 为溶剂， 反应 1.0h， 以89%的产率得到[Re(Br)(CO)3]2(2,2'-bipyrimidine)
  参考文献：
  名称：

  The case of [(bpm)Re(CO)3Br] and anti-[Br(CO)3Re(μ-bpm)Re(CO)3Br] (bpm: 2,2′-bipyrimidine) towards multi-metallic ReI species and their properties

  摘要：

  DOI：

  10.1016/j.poly.2021.115436

文献信息

• Photochemistry and Emission of the Dinuclear Complexes (CO)5MnRe(CO)3(L) (L = 2,2'-Bipyrimidine, 2,3-Bis(2-pyridyl)pyrazine) and Bridged Trinuclear Complexes (CO)5MnRe(CO)3(L)Re(Br)(CO)3 and (CO)5MnRe(CO)3(BPYM)W(CO)4: Effect of the Remote Metal Center on the Photodissociation of the Mn-Re Bond
  作者：J. W. M. van Outersterp、D. J. Stufkens、A. Vlcek

  DOI：10.1021/ic00125a016

  日期：1995.10

  Photochemical and emission properties of the dinuclear (CO)(5)MnRe(CO)(3)(L) and trinuclear (CO)(5)MnRe(CO)(3)(L)Re(Br)(CO)(3) and (CO)(5)MnRe(CO)(3)(BPYM)W(CO)(4) complexes (L = 2,2'-bipyrimidine (BPYM), 2,3-bis(2-pyridyl)pyrazine (DPP)) are described. All these compounds undergo photochemical homolysis of the Mn-Re bond upon excitation into their MLCT absorption band(s) in the visible spectral region. Mn(Cl)(CO)(5) and Re(Cl)(CO)(3)(L) or Re(Cl)(CO)(3)(L)Re(Br)(CO)(3) are formed in chlorinated solvents (CH2Cl2, CCl4) from the former two types of complexes, respectively. In THF, photolysis produces Mn-2(CO)(10), together with [Re(CO)(3)(L)](.), [Re(CO)(3)(L)Re(Br)(CO)(3)](.), or [Re(CO)(3)(BPYM)W(CO)(4)](.) radicals, respectively, which presumably contain also a coordinated THF molecule. Photoreactions of the dinuclear complexes occur with high quantum yields (0.36 for BPYM and 0.54 for DPP), which are independent of the temperature and of the excitation wavelength. The attachment of the Re(Br)(CO)(3) group to the potentially bridging ligand L in (CO)(5)MnRe(CO)(3)(L) to form the L-bridged trinuclear species strongly influences the excited state dynamics involved in the photochemistry. Thus, the photochemical quantum yields of the trinuclear complexes are both temperature and excitation wavelength dependent. The apparent activation energy, together with the overall quantum yield, decreases upon changing the excitation from the high- to the low-energy MLCT absorption band. The Mn-Re bond homolysis is about 6 times more efficient for bridging DPP than for bridging BPYM. The dinuclear complexes exhibit, in a 2-MeTHF glass at 80 K, an emission from thermally unequilibrated states, whereas double emission, extending into the near-IR spectral region, was observed for (CO)(2)MnRe(CO)(3)(DPP)Re(Br)(CO)(3). Its BPYM analogue is nonemissive. To account for this complex photobehavior, an excited state diagram and a qualitative dynamics model are proposed. The reaction is assumed to occur from a 3 sigma pi* state that is nonradiatively populated from the higher MLCT state(s). The main effects of the attachment of the Re(Br)(CO)(3) group, which is responsible for the changed photochemical behavior, are the profound stabilization of the pi* LUMO of the bridging ligand L and the introduction of another MLCT excited state into the trinuclear molecule.